Home Other Building Blocks 1454-53-1
1454-53-1,MFCD01861280
Catalog No.:AA001KSN

1454-53-1 | 1-Benzyl-3-carbethoxy-4-piperidone, HCl

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5g
95%
in stock  
$9.00   $7.00
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10g
95%
in stock  
$12.00   $8.00
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25g
95%
in stock  
$22.00   $15.00
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100g
95%
in stock  
$27.00   $19.00
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500g
95%
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$133.00   $93.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA001KSN
Chemical Name:
1-Benzyl-3-carbethoxy-4-piperidone, HCl
CAS Number:
1454-53-1
Molecular Formula:
C15H20ClNO3
Molecular Weight:
297.7772
MDL Number:
MFCD01861280
SMILES:
CCOC(=O)C1CN(CCC1=O)Cc1ccccc1.Cl
NSC Number:
15156
Properties
Properties
 
Form:
Solid  
MP:
175 °C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
323  
Covalently-Bonded Unit Count:
2  
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
5  
Undefined Atom Stereocenter Count:
1  

Upstream Synthesis Route

[1]BulletinoftheChemicalSocietyofJapan,1958,vol.31,p.418,420

[1]Tetrahedron,1991,vol.50,#2,p.515-528

[2]TetrahedronLetters,2012,vol.53,#26,p.3296-3300

[3]BioorganicandMedicinalChemistry,2018,vol.26,#8,p.1784-1796

[4]ArchivderPharmazie,2018,vol.351,#9,

[5]Patent:CN108586454,2018,A,.Locationinpatent:Paragraph0134;0136;0137

[6]Patent:US2002/19531,2002,A1,

[7]TetrahedronAsymmetry,2004,vol.15,#20,p.3281-3287

[8]JournalofMedicinalChemistry,2013,vol.56,#4,p.1693-1703

[1]Patent:EP1552842,2005,A1,.Locationinpatent:Page/Pagecolumn301

[2]Patent:WO2017/144639,2017,A1,.Locationinpatent:Page/Pagecolumn97

[3]Patent:WO2014/15291,2014,A1,.Locationinpatent:Page/Pagecolumn172

[1]Patent:WO2008/130584,2008,A1,.Locationinpatent:Page/Pagecolumn131;135

[2]OrganicProcessResearchandDevelopment,2011,vol.15,#5,p.1138-1148

[3]BioorganicandMedicinalChemistryLetters,2011,vol.21,#13,p.3970-3975

[4]Patent:WO2011/103091,2011,A1,.Locationinpatent:Page/Pagecolumn93

[1]TetrahedronAsymmetry,2004,vol.15,#20,p.3281-3287

[2]EuropeanJournalofOrganicChemistry,2003,#4,p.721-726

[3]Tetrahedron,1991,vol.50,#2,p.515-528

Downstream Synthesis Route

[1]Morosawa[BulletinoftheChemicalSocietyofJapan,1958,vol.31,p.418,420]Bolyard[JournaloftheAmericanChemicalSociety,1930,vol.52,p.1030]Brookes;Walker[JournaloftheChemicalSociety,1957,p.3173]

[2]Huber,Imre;Zupk,Istvn;Kovcs,IdaJ.;Minorics,Renta;Gulys-Fekete,Gergely;Masz,Gbor;Perjsi,Pl[MonatsheftefurChemie,2015,vol.146,#6,p.973-981]

[1]Moron,Jacqueline;Nguyen,ChiHung;Bisagni,Emile[JournaloftheChemicalSociety.PerkintransactionsI,1983,#2,p.225-229]

[1]Moron,Jacqueline;Nguyen,ChiHung;Bisagni,Emile[JournaloftheChemicalSociety.PerkintransactionsI,1983,#2,p.225-229]

[1]Tetrahedron,1991,vol.50,p.515-528

[2]TetrahedronLetters,2012,vol.53,p.3296-3300

[3]BioorganicandMedicinalChemistry,2018,vol.26,p.1784-1796

[4]ArchivderPharmazie,2018,vol.351

[5]Patent:CN108586454,2018,A.Locationinpatent:Paragraph0134;0136;0137

[6]Patent:US2002/19531,2002,A1

[7]TetrahedronAsymmetry,2004,vol.15,p.3281-3287

[8]JournalofMedicinalChemistry,2013,vol.56,p.1693-1703

1454-53-1    32968-43-7   
7-benzyl-2-(phenoxymethyl)-1,2,6,7,8,9-hexahydro-5H-1,3oxazolo3,2-apyrido3,4-epyrimidin-5-one 
 
7-benzyl-2-(phenoxymethyl)-2,3,6,7,8,9-hexahydro-5H-1,3oxazolo3,2-apyrido4,3-dpyrimidin-5-one 

[1]Forfar,Isabelle;Jarry,Christian;Laguerre,Michel;Leger,Jean-Michel;Pianet,Isabelle[Tetrahedron,1999,vol.55,#44,p.12819-12828]

Literature
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